Veranova: A CDMO that manages complexity with confidence.
01 2Veranova, L.P.
02 6Cambrex Charles City, Inc
03 1Chattem Chemicals, Inc.
04 1Curia New York, Inc.
05 1Siegfried USA, LLC
06 1SpecGx LLC
01 1AMPHETAMINE ASPARTATE
02 3Amphetamine Aspartate
03 1Amphetamine Aspratate Monohydrate
04 5Phenyl-2-(R,S)-Aminopropane Aspartate
05 1Phenyl-2-(R,S)-Aminopropane L-Aspartate
06 1Racemic Amphetamine Aspartate
01 1Ireland
02 1Switzerland
03 10U.S.A
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0061
Start Marketing Date : 1999-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
AMPHETAMINE ASPARTATE MONOHYDRATE
NDC Package Code : 49812-0295
Start Marketing Date : 2021-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AMPHETAMINE ASPARTATE MONOHYDRATE
NDC Package Code : 59116-1960
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-4990
Start Marketing Date : 2015-08-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AMPHETAMINE ASPARTATE MONOHYDRATE
NDC Package Code : 59116-1961
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AMPHETAMINE ASPARTATE MONOHYDRATE
NDC Package Code : 59116-1962
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AMPHETAMINE ASPARTATE MONOHYDRATE
NDC Package Code : 59116-1963
Start Marketing Date : 2013-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AMPHETAMINE ASPARTATE MONOHYDRATE
NDC Package Code : 59116-1964
Start Marketing Date : 2015-09-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-3993
Start Marketing Date : 2013-11-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AMPHETAMINE ASPARTATE MONOHYDRATE
NDC Package Code : 0792-3937
Start Marketing Date : 2023-07-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A ADDERALL XR 10 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ADDERALL XR 10, including repackagers and relabelers. The FDA regulates ADDERALL XR 10 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ADDERALL XR 10 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ADDERALL XR 10 supplier is an individual or a company that provides ADDERALL XR 10 active pharmaceutical ingredient (API) or ADDERALL XR 10 finished formulations upon request. The ADDERALL XR 10 suppliers may include ADDERALL XR 10 API manufacturers, exporters, distributors and traders.
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National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing ADDERALL XR 10 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ADDERALL XR 10 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture ADDERALL XR 10 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain ADDERALL XR 10 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ADDERALL XR 10 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ADDERALL XR 10 suppliers with NDC on PharmaCompass.
We have 6 companies offering ADDERALL XR 10
Get in contact with the supplier of your choice:
